licoricidin
A member of the class of hydroxyisoflavans that is R-isoflavan with hydroxy groups at positions 7, 2' and 4', a methoxy group at position 5 and prenyl groups at positions 6 and 3'. Isolated from Glycyrrhiza uralensis, it exhibits antibacterial activity.
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
Classification
Chemical structure
| Molecular formula | C26H32O5 |
|---|---|
| Charge | 0 |
| Average mass | 424.537 Da |
| Monoisotopic mass | 424.22497 Da |
| Source | ChEBI |
| InChIKey | GBRZTUJCDFSIHM-KRWDZBQOSA-N |
[H][C@@]1(c2ccc(O)c(CC=C(C)C)c2O)COc2cc(O)c(CC=C(C)C)c(OC)c2C1
InChI=1S/C26H32O5/c1-15(2)6-8-19-22(27)11-10-18(25(19)29)17-12-21-24(31-14-17)13-23(28)20(26(21)30-5)9-7-16(3)4/h6-7,10-11,13,17,27-29H,8-9,12,14H2,1-5H3/t17-/m0/s1
Also called
- 4-[(3R)-7-hydroxy-5-methoxy-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-2H-chromen-3-yl]-2-(3-methylbut-2-en-1-yl)benzene-1,3-diol
- 2',4',7'-trihydroxy-5-methoxy-3',6-diisopentenyl-isoflavan
- 4-((R)-7-hydroxy-5-methoxy-6-(3-methyl-but-2-enyl)-1-benzopyran-3-yl)-2-((E)-3-methyl-but-2-enyl)-benzene-1,3-diol
Cross-references
- cas:30508-27-1
- kegg.compound:C16986
- lipidmaps:LMPK12080045
- reaxys:5362788
Activity roles
- antibacterial agent
CHEBI:33282
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:69082 |
licoricidin | antibioticmech:chebi-8caa89d238 |
2026-08-30 |
Curation history
-
SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories